α-Ureidoalkylation of thiosemicarbazide and aminoguanidine View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-05

AUTHORS

A. S. Sigachev, A. N. Kravchenko, P. A. Belyakov, O. V. Lebedev, N. N. Makhova

ABSTRACT

Optimum conditions for the targeted synthesis of 5,7-dialkyl-3-thioxoperhydroimid-azo[4,5-e][1,2,4]triazin-6-ones, 4,5-bis(3-thiosemicarbazido(guanidinoamino))imidazolidin-2-ones, and 1,3-dialkyl-4-(guanidinoimino)imidazolidin-2-ones by α-ureidoalkylation of thiosemicarbazide or aminoguanidine were found. A novel conglomerate in the series of imidazolidin-2-one derivatives was detected: 4,5-bis(guanidinoamino)-1,3-dimethylimid-azolidin-2-one dihydrochloride dihydrate.

PAGES

865-872

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-006-0344-6

DOI

http://dx.doi.org/10.1007/s11172-006-0344-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1052686174


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